JP2004511577A5 - - Google Patents
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- JP2004511577A5 JP2004511577A5 JP2002537727A JP2002537727A JP2004511577A5 JP 2004511577 A5 JP2004511577 A5 JP 2004511577A5 JP 2002537727 A JP2002537727 A JP 2002537727A JP 2002537727 A JP2002537727 A JP 2002537727A JP 2004511577 A5 JP2004511577 A5 JP 2004511577A5
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- JP
- Japan
- Prior art keywords
- compound
- formula
- carbon atom
- subjecting
- iii
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
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- 150000001875 compounds Chemical class 0.000 claims description 74
- 125000004432 carbon atoms Chemical group C* 0.000 claims description 36
- 229910052799 carbon Inorganic materials 0.000 claims description 28
- -1 nitroheterocycle Chemical group 0.000 claims description 17
- 238000006798 ring closing metathesis reaction Methods 0.000 claims description 14
- 230000000707 stereoselective Effects 0.000 claims description 8
- 125000001424 substituent group Chemical group 0.000 claims description 8
- 239000000654 additive Substances 0.000 claims description 6
- 230000000996 additive Effects 0.000 claims description 6
- 125000006575 electron-withdrawing group Chemical group 0.000 claims description 6
- 125000004433 nitrogen atoms Chemical group N* 0.000 claims description 6
- 125000004430 oxygen atoms Chemical group O* 0.000 claims description 6
- 125000004434 sulfur atoms Chemical group 0.000 claims description 6
- 230000003213 activating Effects 0.000 claims description 4
- 230000004913 activation Effects 0.000 claims description 4
- 125000002252 acyl group Chemical group 0.000 claims description 4
- 125000004423 acyloxy group Chemical group 0.000 claims description 4
- 125000005035 acylthio group Chemical group 0.000 claims description 4
- 125000003545 alkoxy group Chemical group 0.000 claims description 4
- 125000004414 alkyl thio group Chemical group 0.000 claims description 4
- 125000004104 aryloxy group Chemical group 0.000 claims description 4
- 125000000051 benzyloxy group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])O* 0.000 claims description 4
- 125000002619 bicyclic group Chemical group 0.000 claims description 4
- 125000004122 cyclic group Chemical group 0.000 claims description 4
- 125000005291 haloalkenyloxy group Chemical group 0.000 claims description 4
- 125000004438 haloalkoxy group Chemical group 0.000 claims description 4
- 125000004996 haloaryloxy group Chemical group 0.000 claims description 4
- 229910052736 halogen Inorganic materials 0.000 claims description 4
- 125000005843 halogen group Chemical group 0.000 claims description 4
- 125000001183 hydrocarbyl group Chemical group 0.000 claims description 4
- 125000004356 hydroxy functional group Chemical group O* 0.000 claims description 4
- 150000003839 salts Chemical class 0.000 claims description 4
- 239000011780 sodium chloride Substances 0.000 claims description 4
- 230000002194 synthesizing Effects 0.000 claims description 4
- 125000003342 alkenyl group Chemical group 0.000 claims description 3
- 125000004442 acylamino group Chemical group 0.000 claims description 2
- 125000006323 alkenyl amino group Chemical group 0.000 claims description 2
- 125000003302 alkenyloxy group Chemical group 0.000 claims description 2
- 125000003282 alkyl amino group Chemical group 0.000 claims description 2
- 125000000217 alkyl group Chemical group 0.000 claims description 2
- 125000004390 alkyl sulfonyl group Chemical group 0.000 claims description 2
- 125000005278 alkyl sulfonyloxy group Chemical group 0.000 claims description 2
- 125000006319 alkynyl amino group Chemical group 0.000 claims description 2
- 125000000304 alkynyl group Chemical group 0.000 claims description 2
- 125000005251 aryl acyl group Chemical group 0.000 claims description 2
- 125000001769 aryl amino group Chemical group 0.000 claims description 2
- 125000003118 aryl group Chemical group 0.000 claims description 2
- 230000027455 binding Effects 0.000 claims description 2
- 230000015572 biosynthetic process Effects 0.000 claims description 2
- 239000003054 catalyst Substances 0.000 claims description 2
- 238000006243 chemical reaction Methods 0.000 claims description 2
- 239000003153 chemical reaction reagent Substances 0.000 claims description 2
- 230000000875 corresponding Effects 0.000 claims description 2
- 230000001808 coupling Effects 0.000 claims description 2
- 238000010168 coupling process Methods 0.000 claims description 2
- 238000005859 coupling reaction Methods 0.000 claims description 2
- 125000004093 cyano group Chemical group *C#N 0.000 claims description 2
- 125000004663 dialkyl amino group Chemical group 0.000 claims description 2
- 150000004985 diamines Chemical class 0.000 claims description 2
- 125000004986 diarylamino group Chemical group 0.000 claims description 2
- 150000002148 esters Chemical class 0.000 claims description 2
- 125000001188 haloalkyl group Chemical group 0.000 claims description 2
- 125000000232 haloalkynyl group Chemical group 0.000 claims description 2
- 125000003106 haloaryl group Chemical group 0.000 claims description 2
- 150000002367 halogens Chemical class 0.000 claims description 2
- 125000000623 heterocyclic group Chemical group 0.000 claims description 2
- 229910052739 hydrogen Inorganic materials 0.000 claims description 2
- 239000001257 hydrogen Substances 0.000 claims description 2
- 125000004435 hydrogen atoms Chemical class [H]* 0.000 claims description 2
- 239000003446 ligand Substances 0.000 claims description 2
- 239000002184 metal Chemical class 0.000 claims description 2
- 229910052751 metal Chemical class 0.000 claims description 2
- 238000000034 method Methods 0.000 claims description 2
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims description 2
- 125000004971 nitroalkyl group Chemical group 0.000 claims description 2
- 125000004999 nitroaryl group Chemical group 0.000 claims description 2
- 238000005935 nucleophilic addition reaction Methods 0.000 claims description 2
- 125000002524 organometallic group Chemical group 0.000 claims description 2
- OAICVXFJPJFONN-UHFFFAOYSA-N phosphorus Chemical class [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 claims description 2
- 229910052698 phosphorus Inorganic materials 0.000 claims description 2
- 239000011574 phosphorus Chemical class 0.000 claims description 2
- 125000003367 polycyclic group Chemical group 0.000 claims description 2
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims description 2
- 125000005017 substituted alkenyl group Chemical group 0.000 claims description 2
- 125000000547 substituted alkyl group Chemical group 0.000 claims description 2
- 125000004426 substituted alkynyl group Chemical group 0.000 claims description 2
- 229910052717 sulfur Inorganic materials 0.000 claims description 2
- 150000003463 sulfur Chemical class 0.000 claims description 2
- 238000003786 synthesis reaction Methods 0.000 claims description 2
- 125000003396 thiol group Chemical group [H]S* 0.000 claims description 2
- DFKDOZMCHOGOBR-NCSQYGPNSA-N Zaragozic acid Chemical compound C([C@@H](C)[C@H](OC(C)=O)C(=C)CC[C@]12[C@H](O)[C@H]([C@](O2)(C(O)=O)[C@@](O)([C@H](O1)C(O)=O)C(O)=O)OC(=O)/C=C/[C@@H](C)C[C@@H](C)CC)C1=CC=CC=C1 DFKDOZMCHOGOBR-NCSQYGPNSA-N 0.000 claims 2
- 239000002253 acid Substances 0.000 claims 2
- 150000001576 beta-amino acids Chemical class 0.000 claims 2
- 150000001371 alpha-amino acids Chemical class 0.000 claims 1
- 235000008206 alpha-amino acids Nutrition 0.000 claims 1
- 230000000694 effects Effects 0.000 claims 1
- 150000002772 monosaccharides Chemical class 0.000 claims 1
- 229920001542 oligosaccharide Polymers 0.000 claims 1
- 150000002482 oligosaccharides Polymers 0.000 claims 1
- STECJAGHUSJQJN-USLFZFAMSA-N scopolamine Chemical compound C1([C@@H](CO)C(=O)OC2C[C@@H]3N([C@H](C2)[C@@H]2[C@H]3O2)C)=CC=CC=C1 STECJAGHUSJQJN-USLFZFAMSA-N 0.000 claims 1
- 229930004668 tropane alkaloids Natural products 0.000 claims 1
- 239000000126 substance Substances 0.000 description 6
- 125000000262 haloalkenyl group Chemical group 0.000 description 1
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| AUPR1057A AUPR105700A0 (en) | 2000-10-27 | 2000-10-27 | Process for preparation of bicyclic and polycyclic molecules |
| PCT/AU2001/001379 WO2002034736A1 (fr) | 2000-10-27 | 2001-10-26 | Procede de preparation de molecules bicycliques et polycycliques |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JP2004511577A JP2004511577A (ja) | 2004-04-15 |
| JP2004511577A5 true JP2004511577A5 (fr) | 2005-12-22 |
Family
ID=3825101
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2002537727A Pending JP2004511577A (ja) | 2000-10-27 | 2001-10-26 | 二環式及び多環式分子の調製方法 |
Country Status (7)
| Country | Link |
|---|---|
| US (1) | US7012142B2 (fr) |
| EP (1) | EP1334092B1 (fr) |
| JP (1) | JP2004511577A (fr) |
| AU (2) | AUPR105700A0 (fr) |
| CA (1) | CA2427021A1 (fr) |
| DE (1) | DE60128382D1 (fr) |
| WO (1) | WO2002034736A1 (fr) |
Families Citing this family (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| KR101620137B1 (ko) * | 2013-06-14 | 2016-05-12 | 주식회사 엘지화학 | 플러렌 유도체의 제조 방법 |
| TW202322824A (zh) | 2020-02-18 | 2023-06-16 | 美商基利科學股份有限公司 | 抗病毒化合物 |
| EP4323362A1 (fr) | 2021-04-16 | 2024-02-21 | Gilead Sciences, Inc. | Procédés de préparation de carbanucléosides à l'aide d'amides |
Family Cites Families (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5770180A (en) * | 1992-08-24 | 1998-06-23 | Organix, Inc. | Bridge-substituted tropanes for methods of imaging and therapy |
| US5948933A (en) * | 1997-07-11 | 1999-09-07 | Organix, Inc. | Tropane analogs and methods for inhibition of monoamine transport |
-
2000
- 2000-10-27 AU AUPR1057A patent/AUPR105700A0/en not_active Abandoned
-
2001
- 2001-10-26 AU AU1364302A patent/AU1364302A/xx not_active Withdrawn
- 2001-10-26 DE DE60128382T patent/DE60128382D1/de not_active Expired - Lifetime
- 2001-10-26 EP EP01981942A patent/EP1334092B1/fr not_active Expired - Lifetime
- 2001-10-26 WO PCT/AU2001/001379 patent/WO2002034736A1/fr active IP Right Grant
- 2001-10-26 JP JP2002537727A patent/JP2004511577A/ja active Pending
- 2001-10-26 CA CA002427021A patent/CA2427021A1/fr not_active Abandoned
-
2003
- 2003-04-25 US US10/423,563 patent/US7012142B2/en not_active Expired - Fee Related
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